Ankle sprain, Prevention, App, implementation, Cost-effectiveness, Compliance, Enkelverstuiking, Preventie, Implementatie, Kosten-effectiviteitsanalyse, Compliantie
Conditions
Interventions
After subjects have finished ankle sprain treatment by means of usual care, they will be randomized to any of the two study groups. Subjects allocated to the 'regular' intervention group will receive
Sponsors
EMGO Institute for Health and Care research of the VU University Medical Center
VeiligheidNL
Eligibility
Inclusion criteria
Inclusion criteria: Individuals who have sustained an ankle sprain within the past two months, and who are currently being treated for that injury by either a physiotherapist, physician, sports physician, or orthopedic surgeon are eligible for inclusion.
Exclusion criteria
Exclusion criteria: None
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcome measures include injury recurrence incidence, costs of injury (and cost-effectiveness of the intervention), as well as barriers and facilitators towards the use of the eight-week training program, including knowledge and attitude regarding the prevention of ankle sprain recurrences. | — |
Primary
| Measure | Time frame |
|---|---|
| Primary outcome measures will be compliance to the prescribed eight-week program. | — |
Contacts
Public ContactEvert Verhagen
Department of Public and Occupational Health VU University Medical Center Van der Boechorststraat 7
Outcome results
None listed